Histiocytosis X: A seven-year experience at a children's hospital von Burton Esterly, Nancy, Maurer, Helen S., Gonzalez-Crussi, Frank

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Chromosome abnormalities in tumor cells from patients with sporadic Wilmś tumor von KONDO, K, CHILCOTE, R. R, MAURER, H. S, ROWLEY, J. D

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Therapy-Related Myelodysplastic Syndrome and Acute Myeloid Leukemia in Children: Correlation Between Chromosomal Abnormalities and Prior Therapy von Rubin, Charles M., Arthur, Diane C., Woods, William G., Lange, Beverly J., Nowell, Peter C., Rowley, Janet D., Nachman, James, Bostrom, Bruce, Baum, Edward S., Suarez, Carlos R., Shah, Narayan R., Morgan, Elaine, Maurer, Helen S., McKenzie, Steven E., Larson, Richard A., Le Beau, Michelle M.

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Dependence of the Oxygen Affinity of Blood on the Presence of Foetal or Adult Haemoglobin von MAURER, HELEN S, BEHRMAN, RICHARD E, HONIG, GEORGE R

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Hepatoblastoma. Attempt at characterization of histologic subtypes von González-Crussi, F, Upton, M P, Maurer, H S

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Single copies of the N‐myc oncogene in neuroblastomas from children presenting with the syndrome of opsoclonus‐myoclonus von Cohn, Susan L., Salwen, Helen, Herst, C. V., Maurer, Helen S., Nieder, Michael L., Morgan, Elaine R., Rosen, Steven T.

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Chromosome Pattern in Childhood Acute Nonlymphocytic Leukemia (ANLL) von Kaneko, Yasuhiko, Rowley, Janet D., Maurer, Helen S., Variakojis, Daina, Moohr, John W.

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Epstein-Barr virus-induced diseases in boys with the X-linked lymphoproliferative syndrome (XLP): Update on studies of the registry von Purtilo, David T., Sakamoto, Kiyoshi, Barnabei, Vanessa, Seeley, Janet, Bechtold, Thomas, Rogers, Geraldine, Yetz, Joanne, Harada, Shinji, Berkel, Izet, Brooks, Carter, Bucchanan, George, Collins, Robert, Cruzi, Frank, Finkelstein, Gerald, Glomstein, Anders, Greally, John, Grunet, Margaret, Henle, Gertrude, Henle, Werner, Kaplan, Elvin, Klein, George, Klemperer, Martin, Landing, Benjamin, Lie, Sevre, Maier, Robert, Maurer, Helen S., Medici, Michael, Ochs, Hans, Pachman, Lauren, Pattengale, Paul, Pearson, Gary, Provisor, Arthur, Vawter, Gordon

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Septic arthritis in two teenaged hemophiliacs von Scott, John Paul, Maurer, Helen S., Dias, Luciano

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Acquired von Willebrand disease in a patient with Wilms tumor von Noronha, Peter A., Hruby, Marilyn A., Maurer, Helen S.

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Methotrexate encephalopathy. A neuropathologic study von Liu, H M, Maurer, H S, Vongsvivut, S, Conway, J J

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H. INFLUENZA B IMMUNIZATION OF CHILDREN WITH SICKLE CELL DISEASES von Frank, Arthur L, Labotka, Richard J, Frisone, Lisa R, Rao, Sudha, McVerry, Patrick H, Samuelson, Joel S, Maurer, Helen S, Yogev, Ram

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Malignant lymphoma of the small intestine in multiple family members.Association with an immunologic deficiency von Maurer, Helen S., Gotoff, Samuel P., Allen, Lawrence, Bolan, James

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The role of genetic factors in the etiology of wilms' tumor. Two pairs of monozygous twins with congenital abnormalities (Aniridia; hemihypertrophy) and discordance for wilms' tumo... von Maurer, Helen S., Pendergrass, Thomas W., Borges, Wayne, Honig, George R.

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X-Linked Lymphoproliferative Syndrome Registry report von Hamilton, Janet K., Paquin, Louise A., Sullivan, John L., Maurer, Helen S., Cruzi, Frank G., Provisor, Arthur J., Philip Steuber, C., Hawkins, Edith, Yawn, David, Cornet, Jo Ann, Clausen, Kathryn, Finkelstein, Gerald Z., Landing, Benjamin, Grunnet, Margaret, Purtilo, David T.

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Malignant lymphoma of the small intestine in multiple family members. Association with an immunologic deficiency von Maurer, Helen S., Gotoff, Samuel P., Allen, Lawrence, Bolan, James

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The role of genetic factors in the etiology of wilms' tumor.Two pairs of monozygous twins with congenital abnormalities (Aniridia; hemihypertrophy) and discordance for wilms' tumor von Maurer, Helen S., Pendergrass, Thomas W., Borges, Wayne, Honig, George R.

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Similarities of the Erythrocytes in Juvenile Chronic Myelogenous Leukemia to Fetal Erythrocytes von Maurer, Helen S., Vida, Loyda N., Honig, George R.

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Methotrexate encephalopathy von Mei Liu, H., Maurer, Helen S., Vongsvivut, Sopa, Conway, James J.

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Hyperthyroidism in an infant with McCune-Albright syndrome: Report of a case with myeloid metaplasia von Samuel, Shantharaj, Gilman, Sherwin, Maurer, Helen S., Rosenthal, Ira M.

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